Karakaya, C. Et Al. 2022. Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified.. The journal of obstetrics and gynaecology research , vol.48 , 1202-1211.

Karakaya, C., Çil, A. P., Bilguvar, K., Çakir, T., Karalok, M. H., Karabacak, R. O., ... Caglayan, A. O.(2022). Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified.. The journal of obstetrics and gynaecology research , vol.48, 1202-1211.

Karakaya, Cengiz Et Al. "Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified.," The journal of obstetrics and gynaecology research , vol.48, 1202-1211, 2022

Karakaya, Cengiz Et Al. "Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified.." The journal of obstetrics and gynaecology research , vol.48, pp.1202-1211, 2022

Karakaya, C. Et Al. (2022) . "Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified.." The journal of obstetrics and gynaecology research , vol.48, pp.1202-1211.

@article{article, author={Cengiz Karakaya Et Al. }, title={Further delineation of familial polycystic ovary syndrome (PCOS) via whole-exome sequencing: PCOS-related rare FBN3 and FN1 gene variants are identified.}, journal={The journal of obstetrics and gynaecology research}, year=2022, pages={1202-1211} }